Thromb Haemost 1967; 17(03/04): 585-594
DOI: 10.1055/s-0038-1654183
Originalarbeiten - Original Articles - Travaux Originaux
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Coagulation Factors in Pregnant Women and Premature Infants with and without the Respiratory Distress Syndrome[*]

Marguerite Markarian M. D.**
1   Department of Pediatrics, University of Colorado Medical Center, Denver, Colorado and the Department of Obstetrics, Hospital San Borja, University of Chile, Santiago (Chile)
,
Annabelle Lindley
1   Department of Pediatrics, University of Colorado Medical Center, Denver, Colorado and the Department of Obstetrics, Hospital San Borja, University of Chile, Santiago (Chile)
,
Jacqueline J. Jackson B. A.,
1   Department of Pediatrics, University of Colorado Medical Center, Denver, Colorado and the Department of Obstetrics, Hospital San Borja, University of Chile, Santiago (Chile)
,
Anne Bannon M. D.
1   Department of Pediatrics, University of Colorado Medical Center, Denver, Colorado and the Department of Obstetrics, Hospital San Borja, University of Chile, Santiago (Chile)
› Author Affiliations
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Publication History

Publication Date:
26 June 2018 (online)

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Summary

Coagulation factors (accelerator globulin, antihemophilic globulin, specific prothrombin, proconvertin complex and Stuart-Prower factor) in 82 low birth weight infants (750–1750 g), 22 normal adult controls and 38 pregnant women prior to delivery were studied at San Borja Hospital in Santiago, Chile.

Pregnant women prior to delivery had significantly higher values of accelerator globulin, antihemophilic globulin, proconvertin complex and Stuart-Prower factor than adult controls, but there was no difference in specific prothrombin.

The coagulation factors were similar in premature infants without RDS as compared to those with RDS (lived and died combined). However, premature infants with RDS who lived had higher values of prothrombin, proconvertin complex, Stuart-Prower factor at 25 hrs and accelerator globulin at 55 hrs of age than those with RDS who died. Most of these findings could be explained by impaired liver function in association with hypoxia.

* Supported in part by grants-in-aid from the University of Colorado Fluid Research Committee, OTH Grant (HE 06684) and NIH Grant (HD 23584).


** Dr. Markarian performed this study during the tenure of a USPHS Postdoctoral Research Fellowship.